Licensed Practical Nurse
- AB, Canada
- Edmonton, AB, Canada
Classification: Licensed Practical Nurse Union: AUPE AUX Unit and Program: Clinical Trial Unit Primary Location: U of A Hospital Location Details: As Per Location Multi-Site: Not Applicable FTE: 1.00 Posting End Date: 12-NOV-2026 Employee Class: Regular Full Time Date Available: 07-DEC-2026 Hours per Shift: 7.75 Length of Shift in weeks: 2 Shifts per cycle: 10 Shift Pattern: Days Days Off: Saturday/Sunday Minimum Salary: $33.16 Maximum Salary: $43.42 Vehicle Requirement: Not Applicable · Full-time
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Job details
- Pay
- Classification: Licensed Practical Nurse Union: AUPE AUX Unit and Program: Clinical Trial Unit Primary Location: U of A Hospital Location Details: As Per Location Multi-Site: Not Applicable FTE: 1.00 Posting End Date: 12-NOV-2026 Employee Class: Regular Full Time Date Available: 07-DEC-2026 Hours per Shift: 7.75 Length of Shift in weeks: 2 Shifts per cycle: 10 Shift Pattern: Days Days Off: Saturday/Sunday Minimum Salary: $33.16 Maximum Salary: $43.42 Vehicle Requirement: Not Applicable
- Job type
- Full-time
- Apply by
- Posting language
- English
- Posted
Original job description
The Alberta Health Services Clinical Trials Unit (AHS-CTU) is currently recruiting a Licensed Practical Nurse (LPN) to support Investigators in the conduct of clinical trials. The key responsibilities are: Support study management activities, including the screening and recruitment of potential study participants. Obtain informed consent from participants in compliance with ethical and regulatory standards. Perform protocol-specific procedures, such as collecting biological samples (blood, urine), obtaining vital signs and completing relevant study assessments. Coordinate and organize participant visits and follow-up appointments in accordance with study protocols. Provide participant education and counseling related to study participation, visit schedules, and data collection procedures. Dispense and document study medication in accordance with protocol requirements and applicable regulations. Perform accurate and timely data entry and documentation in study databases and participant records. Assist in the development, review, and maintenance of study-specific source documents and case report forms. Review and file study-related correspondence and documentation within the Investigator Site File (ISF).Collaborate with research and clinical team members to ensure study activities are conducted efficiently, accurately, and ethically. Working under limited supervision, you will perform diversified duties requiring independent judgement and confidentiality. To be successful in this role, you will require excellent problem-solving skills and the ability to work in a team environment. You must be able to handle multiple demands with short timelines while remaining sufficiently flexible to accept new workloads as necessary.
Description:
As a Licensed Practical Nurse (LPN), you are part of an interprofessional health care team, utilizing nursing processes, critical thinking, problem solving, and decision making skills. You will be guided by your education, experience, and demonstrated skill level, in alignment with applicable legislation, standards of practice, policies, and procedures. You will play a key role in providing safe, high quality, patient and family centred care while reflecting the organization's shared vision and values.
Classification: Licensed Practical Nurse Union: AUPE AUX Unit and Program: Clinical Trial Unit Primary Location: U of A Hospital Location Details: As Per Location Multi-Site: Not Applicable FTE: 1.00 Posting End Date: 12-NOV-2026 Employee Class: Regular Full Time Date Available: 07-DEC-2026 Hours per Shift: 7.75 Length of Shift in weeks: 2 Shifts per cycle: 10 Shift Pattern: Days Days Off: Saturday/Sunday Minimum Salary: $33.16 Maximum Salary: $43.42 Vehicle Requirement: Not Applicable
Required Qualifications:
Completion of an accredited practical nurse education program. Active or eligible for registration and a practice permit as a Licensed Practical Nurse with the College of LPNs and HCAs of Alberta (CLHA). Current Basic Cardiac Life Support - Health Care Provider (BCLS-HCP).
Additional Required Qualifications:
Minimum 2–3 years of current experience hands on experience in pharmaceutical clinical research, supporting (Phases I–IV) clinical trials in Cardiology and Pulmonary therapeutic research. Proven expertise in all aspects of study coordination and participant management, including pre-screening, screening, participant recruitment, informed consent, enrollment, retention, and follow-up activities. Comprehensive knowledge of clinical trial regulations and guidelines, including ICH-GCP, Health Canada, and FDA requirements. Proficiency in electronic data capture (EDC) systems and clinical trial databases, including iMedidata and Redcap. Strong problem-solving, critical thinking, and organizational skills with the ability to manage multiple priorities and tight timelines and accept new workloads as necessary. Demonstrated ability to work effectively both independently and as part of a multidisciplinary research team, with the ability to build positive relationships with research participants, investigators, and team members. Must be able to lift and transport large volumes of charts, binders, lab kits, boxes etc to various areas on a regular basis, and push/pull loaded carts. Physical demands of the job include sitting for extended periods, lifting and transporting office/medical supplies and equipment weighing up to 40 lbs., and using repetive motions, lifting, bending, reaching and standing for prolonged periods.
Preferred Qualifications:
Health Canada Division 5, GCP certification. Current experience in using Connect Care and Netcare. Clinical Research Coordinator training through CITI. Experience in creating source documents. Phlebotomy skills and experience in specimen collection and handling. Skilled in standard computer applications (Microsoft Excel, Word, PowerPoint). Proven ability to perform diversified duties requiring independent judgment, discretion, and confidentiality.
More about this job
Responsibilities
Support clinical trial investigators by coordinating participant screening, recruitment, consent, visits, follow-up, education, and protocol-specific assessments. Dispense and document study medication, collect specimens, maintain study records and databases, and collaborate with research and clinical teams to ensure ethical and accurate trial conduct.
Requirements
Requires completion of an accredited practical nursing program, active or eligible Alberta LPN registration, current BCLS-HCP, and 2–3 years of hands-on pharmaceutical clinical research experience supporting Phase I–IV cardiology and pulmonary trials. Candidates need clinical trial coordination expertise, knowledge of ICH-GCP and regulatory requirements, proficiency with EDC systems such as iMedidata and REDCap, and the ability to manage competing priorities and physical demands.
Skills
- Clinical Trial Coordination
- Participant Screening And Recruitment
- Informed Consent
- Participant Management
- Clinical Trial Regulations
- ICH-GCP
- Health Canada And FDA Requirements
- Electronic Data Capture
- iMedidata
- REDCap
- Specimen Collection
- Phlebotomy
- Study Medication Dispensing
- Clinical Documentation
- Critical Thinking
- Problem-Solving
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Science & Research
Keywords
- Licensed Practical Nurse
- Clinical Trials
- Clinical Research
- Phase I–IV Trials
- Cardiology
- Pulmonary Research
- Study Coordination
- Participant Screening
- Participant Recruitment
- Informed Consent
- Participant Enrollment
- Participant Retention
- ICH-GCP
- Health Canada
- FDA Requirements
- Electronic Data Capture
- iMedidata
- REDCap
- Connect Care
- Netcare
- CITI Clinical Research Coordinator Training
- Health Canada Division 5
- BCLS-HCP
- Phlebotomy
- Specimen Collection
- Source Documents
- Case Report Forms
- Investigator Site File
- Microsoft Excel
- Microsoft Word